PMID- 35004790 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20220111 IS - 2296-858X (Print) IS - 2296-858X (Electronic) IS - 2296-858X (Linking) VI - 8 DP - 2021 TI - Exacerbation of Psoriasis Following COVID-19 Vaccination: Report From a Single Center. PG - 812010 LID - 10.3389/fmed.2021.812010 [doi] LID - 812010 AB - The temporal association had been reported between vaccination and exacerbation of psoriasis, and episodes of psoriasis flare-up have recently been attributed to COVID-19 vaccines. We recruited 32 unimmunized controls and 51 vaccinated psoriasis patients, 49 of whom were under biological therapy, with regular clinic visits receiving a total of 63 shots of vaccines, including 30 doses of Moderna mRNA-1273 and 33 doses of AstraZeneca-Oxford AZD1222. Fifteen episodes of exacerbation attacked within 9.3 +/- 4.3 days, which is higher than two episodes in the control group (p = 0.047). The mean post-vaccination severity of the worsening episodes increased from PASI 3.1 to 8.0 (p < 0.001). Three patients showed morphologic change from chronic plaque-type to guttate psoriasis. Deterioration of psoriasis following COVID-19 vaccination was not associated with age, sex, disease duration, psoriatic arthritis, family history of psoriasis, history of erythroderma, current biologics use, comorbidities, vaccine types, human leukocyte antigen (HLA)-C genotypes, baseline PASI nor pre-vaccination PASI. For those who received two doses of vaccination, all but one patient aggravated after the first shot but not the second. The mechanism of psoriasis exacerbation in immunized individuals is unclear, but Th17 cells induced by COVID-19 vaccines may play a role. In the pandemic era, psoriasis patients and physicians should acknowledge the possibility of fluctuation of disease activity when vaccinated against COVID-19. Nevertheless, compared to a treatable dermatologic disease with rapid resolution of exacerbation, psoriasis patients who do not have contraindications to vaccination should benefit from COVID-19 vaccines in the prevention of severe COVID-19 infection and fatality. CI - Copyright (c) 2021 Huang and Tsai. FAU - Huang, Yi-Wei AU - Huang YW AD - Department of Dermatology, National Taiwan University Hospital, Taipei, Taiwan. FAU - Tsai, Tsen-Fang AU - Tsai TF AD - Department of Dermatology, National Taiwan University Hospital, Taipei, Taiwan. AD - Department of Dermatology, College of Medicine, National Taiwan University, Taipei, Taiwan. LA - eng PT - Journal Article DEP - 20211223 PL - Switzerland TA - Front Med (Lausanne) JT - Frontiers in medicine JID - 101648047 PMC - PMC8733241 OTO - NOTNLM OT - COVID-19 OT - HLA OT - Th17 OT - biologics OT - exacerbation OT - human leukocyte antigen OT - psoriasis OT - vaccine COIS- T-FT has conducted clinical trials or received honoraria for serving as a consultant for Abbvie, Boehringer Ingelheim, Bristol-Myers Squibb, Celgene, Eli-Lilly, Galderma, Janssen-Cilag, Merck Sharp and Dohme, Novartis International AG, Pfizer Inc., and UCB Pharma. However, none of the above has direct conflict regarding this manuscript. The remaining author declares that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. EDAT- 2022/01/11 06:00 MHDA- 2022/01/11 06:01 PMCR- 2021/12/23 CRDT- 2022/01/10 09:26 PHST- 2021/11/09 00:00 [received] PHST- 2021/12/06 00:00 [accepted] PHST- 2022/01/10 09:26 [entrez] PHST- 2022/01/11 06:00 [pubmed] PHST- 2022/01/11 06:01 [medline] PHST- 2021/12/23 00:00 [pmc-release] AID - 10.3389/fmed.2021.812010 [doi] PST - epublish SO - Front Med (Lausanne). 2021 Dec 23;8:812010. doi: 10.3389/fmed.2021.812010. eCollection 2021.